OPTIMAL BALANCE PHARMACY Recall
OPTIMAL BALANCE PHARMACY is recalling Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & …
OPTIMAL BALANCE PHARMACY
Drug & Medication recalls
The newest FDA drug and medication recalls, prescription and over the counter, in plain English. We list the affected lot numbers, the reason for each recall, and whether you should stop taking the product or return it.
178 recalls · updated Sep 17, 2026
Shoolin Pharma Sildenafil Citrate Recall
Shoolin Pharma Chem LLP has recalled a bulk sildenafil citrate powder used for prescription compounding due to manufacturing process deviations found during FDA …
Shoolin Pharma Chem LLP
Datex-Ohmeda, Inc. Recall
Datex-Ohmeda, Inc. is recalling Et Control, Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents, …
Datex-Ohmeda, Inc.
Datex-Ohmeda, Inc. Recall
Datex-Ohmeda, Inc. is recalling Aisys CS2 with Et Control, Datex-Ohmeda anesthesia system, Part Number 1011-9000-000. Hazard: Anesthesia Delivery Systems …
Datex-Ohmeda, Inc.
Diagnostica Stago, Inc. Recall
Diagnostica Stago, Inc. is recalling STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor …
Diagnostica Stago, Inc.
Apollo Care Semaglutide Recall
Apollo Care is recalling Semaglutide 7.5mg multi-dose vials because they may contain tiny particles of nylon and silk material. Injecting this product could …
Apollo Care, LLC
American Regent, Inc. Recall
American Regent, Inc. is recalling Cyanocobalamin injection USP, 10,000 mcg/10 mL (1,000 mcg/mL), For IM or SC Use Only, packaged in a) 10 mL Multi-Dose Vial …
American Regent, Inc.
M.G. Foods Spicy Breakfast Burrito Recall
M.G. Foods is recalling Spicy Breakfast Burritos sold under the Fresh & Ready Foods and Sprig & Sprout brand names because the sausage inside contains soy that …
M.G. Foods, Inc.
Naropin Ropivacaine 0.5% Recall
Fresenius Kabi is recalling Naropin (ropivacaine hydrochloride injection) 0.5%, 20 mL single-dose vials because hair was found in some products. Use of …
Fresenius Kabi USA, LLC
Dabigatran Etexilate 75 mg Recall
Dabigatran Etexilate Capsules, 75 mg, 60-count blister packs are being recalled because stability testing found impurities that exceeded acceptable limits. The …
Ascend Laboratories, LLC
Ascend Dabigatran Etexilate 75mg Recall
Dabigatran Etexilate 75 mg capsules are being recalled because impurities in the drug exceeded safe limits during stability testing. The medication may not work …
Ascend Laboratories, LLC
Rohto Cooling Eye Drops Recall
Rohto Cooling Eye Drops Max Strength (0.4 FL OZ / 13 mL bottles) has been recalled because the manufacturer cannot confirm the product is sterile. Using …
Rohto-Mentholatum (Vietnam) Co., Ltd.
Rohto Cooling Eye Drops Recall
Rohto Cooling Eye Drops Cool Relief has been recalled because the manufacturer cannot guarantee the product is sterile. Use of non-sterile eye drops can lead to …
Rohto-Mentholatum (Vietnam) Co., Ltd.
Major Pharmaceuticals Levothyroxine Recall
Major Pharmaceuticals is recalling Levothyroxine Sodium 88 mcg tablets because they are subpotent, meaning they contain less active ingredient than labeled. …
Major Pharmaceuticals
Major Pharmaceuticals Levothyroxine 75mcg Recall
Major Pharmaceuticals' Levothyroxine Sodium Tablets, USP 75 mcg, have been found to be subpotent, meaning they contain less active ingredient than stated. …
Major Pharmaceuticals
Major Pharmaceuticals Levothyroxine 150 mcg Recall
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets 150 mcg because some batches contain less active ingredient than labeled, which means they may …
Major Pharmaceuticals
Trokendi XR Topiramate 25mg Recall
Trokendi XR 25mg capsules are being recalled because some batches failed to meet dissolution specifications, meaning the capsules may not release the medication …
Supernus Pharmaceuticals, Inc.
CLEVIPREX Clevidipine Recall
Chiesi USA is recalling CLEVIPREX (clevidipine) injectable emulsion vials because the manufacturer cannot assure the product remains sterile. This injectable …
Chiesi USA, Inc.
Victory Medical Glutathione 200mg/mL Injection Recall
Victory Medical Center Pharmacy is recalling its injectable Glutathione 200 mg/mL, 30 mL multi-dose vials because testing found bacterial endotoxin levels …
Victory Medical Center Pharmacy
QC Quality Choice Carbamide Peroxide Recall
QC Quality Choice Carbamide Peroxide 6.5% oral rinse is being recalled because it is sub-potent: it contains far less active ingredient than labeled (about 0.6% …
Bell Pharmaceuticals, Inc
Clinere Carbamide Peroxide Recall
Clinere Carbamide Peroxide ear drops are significantly weaker than labeled and have an unusually low pH, reducing effectiveness and potentially causing …
Bell Pharmaceuticals, Inc
Lupin Glucagon Emergency Kit Recall
Lupin Pharmaceuticals is recalling Glucagon Emergency Kits due to a manufacturing defect that may affect the syringe's ability to inject properly. If you rely …
Lupin Pharmaceuticals Inc.
Medline Industries, LP Recall
Medline Industries, LP is recalling Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model …
Medline Industries, LP
BD ChloraPrep Hi-Lite Orange Recall
BD ChloraPrep Hi-Lite Orange applicators (a skin antiseptic) were distributed without proper sterilization assurance. These products should have been sterilized …
CareFusion 213, LLC
Methohexital Sodium Injection Recall
Methohexital Sodium for Injection 500 mg multiple dose vials made by OneSource Specialty Pharma have failed quality tests for impurities and degradation. …
ONESOURCE SPECIALTY PHARMA LIMITED
Lacosamide Tablets 100mg Recall
Lacosamide 100mg tablets made by Camber Pharmaceuticals may contain a different medication, Selexipag 1000 mcg, mixed into the bottle. Taking the wrong drug by …
Annora Pharma Private Limited
Gas-X Extra Strength Simethicone 125 mg Recall
Gas-X Extra Strength Simethicone 125 mg softgels have been recalled because a machine leak during packaging may have contaminated the capsules with a diluted …
Haleon US Holdings LLC
Corlanor Ivabradine 7.5mg Recall
Corlanor (ivabradine) 7.5mg tablets in 60-count bottles are being recalled due to the presence of a foreign substance. If you take this medication, stop and …
Amgen, Inc.
Corlanor Ivabradine 5mg Recall
Corlanor (ivabradine) 5 mg tablets are being recalled because bottles may contain a foreign substance. If you take this medication, stop and contact your …
Amgen, Inc.
Rapidol Triple Antibiotic Ointment Recall
Rapidol Triple Antibiotic First Aid Ointment is being recalled because the manufacturer did not follow proper manufacturing standards during production. The FDA …
Dabur India Limited
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